Product Recalls in Illinois
Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,932 recalls have been distributed to Illinois in the last 12 months.
Showing 5541–5560 of 30,032 recalls
Recalled Item: Liberty Select Cycler Recalled by Fresenius Medical Care Holdings, Inc. Due...
The Issue: Affected Liberty Select cyclers may display an incorrect time stamp on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection Needle Recalled by Karl Storz Endoscopy Due to The efficacy of the...
The Issue: The efficacy of the manual cleaning process cannot be assured for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Potential...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Initial System Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Power/Pulsar Recalled by Philips North America Llc Due to...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips North America Llc Due to Potential component...
The Issue: Potential component failure in the Gradient Coil could product smoke and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Processing Module The Alinity c Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Processing Module 02P24-02 02P24-40 01R24-56 01R25-56...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Blood Analysis System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott CELL-DYN Ruby Recalled by Abbott Laboratories Due to The devices...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Clean Stool Transportation System-For the collection...
The Issue: Due to a manufacturing defect, certain Para-Pak vials may be at risk for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Para-Pak Zn-PVA/10% Formalin-for the routine collection Recalled by Meridian...
The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.